G-protein coupled receptor 22 transformed cell lines and uses therefor

ABSTRACT

Disclosed herein are cell lines transformed to express G-Protein Coupled Receptor GPCR22 and uses thereof for identifying guanosine analogues and/or other ligands to the receptor. In particular, techniques for transforming  Drosophila  Schneider 2 cells and human astrocytoma 1321N1 cell to express GPCR22 are disclosed as well as transformed cells lines. The transformed cell lines of the instant disclosure may be useful in identifying guanosine analogues and functional equivalents thereof.

RELATED APPLICATIONS

The present application is a U.S. Continuation application which claims benefit of priority to International Patent Application serial number PCT/CA2015/050326 entitled “G-Protein Couple Receptor 22 Transformed Cell Lines and Uses Therefor”, filed Apr. 20, 2015 which in turn claims benefit of priority to U.S. Provisional Patent Application Ser. No. 61/984,618 entitled “G-Protein Coupled Receptor 22 Transformed Cell Lines And Uses Therefor”, filed Apr. 25, 2014 and, U.S. Provisional Patent Application Ser. No. 61/985,373 entitled “G-Protein Coupled Receptor 22 Transformed Cell Lines And Uses Therefor”, filed Apr. 28, 2014, the subject matter of which are herein incorporated by reference.

TECHNICAL FIELD

The present disclosure relates to transfected cell and cell lines transformed to express G-Protein Coupled Receptor 22 and uses therefor.

BACKGROUND

Extracellular guanosine, like adenosine, has been shown to have a plurality of physiological effects both in vitro and in vivo. It affects the growth, differentiation and survival of various cells (Di lorio P, Benfenati et al. 2004, 2006; Ballerini et al., 2006; Tavares et al., 2005; Molz et al., 2005, Rathbone et al., 2008). Guanine-based purinergic signalling has been particularly investigated in the nervous system. For example, exogenously added guanosine stimulates the division of certain cells in culture including astrocytes, fibroblasts and certain tumour cells, including brain tumour cells (Rathbone et al., 1990; Kim et al., 1991; Ciccarelli et al., 2000; Su et al., 2009; 2010; 2013; Jiang et al., 2006; Rathbone et al. NNNA 2008). It promotes differentiation of fetal neurons (Rathbone et al., 1999; 2008) and PC12 cells, stimulates outgrowth of nerve processes (neurites) (Gysbers and Rathbone, 1992; 1996; Bau et al., 2005; Di lorio et al., 2002). Guanosine also prevents apoptosis in astrocytes induced by several stimuli (Pettifer et al., 2004; 2007; Jiang et al., 2007; Su et al., 2009). Furthermore, Guanosine has been shown to protect the CNS from insults such as hypoxia-ischemia (Moretto et al., 2009; Thauerer et al., 2012; Thomazi et al., 2008; zur Nedden et al., 2008), stroke (Chang et al., 2008; Connell et al., 2013; Rathbone et al., 2011), spinal cord injury (Jiang et al., 2008a; Jiang et al., 2007; Jiang et al., 2003a; Sam, 2004), and seizure (Schmidt et al., 2005; Schmidt et al., 2000; Soares et al., 2004), and Parkinson's Disease (Giuliani et al., 2012; Su et al., 2009).

Extracellular guanosine is known to stimulate the synthesis and release of several growth factors from cells, which promotes, for example, astrocyte proliferation (Rathbone et al., 1990; Kim et al., 1991; Ciccarelli et al., 2000), partly by stimulating small numbers of microglia in the astrocyte cultures to produce soluble factors, such as IL-1 (Ciccarelli et al., 2000). Additionally, guanosine promotes the synthesis and release of several potentially neuroprotective trophic factors from a variety of cells, including nerve growth factor (NGF) from astrocytes (Middlemiss et al., 1995) as well as basic fibroblast growth factor (FGF/FGF-2) (Su et al., 2009) and transforming growth factor-□ (TGF-□) (Di lorio et a, 2001). It has been recently shown that exogenous Guanosine can increase intracellular cyclic GMP concentrations through activation of the enzymes hemeoxygenase-1 and hemeoxygenase-2 (HO-1 and HO-2) (Bau et al., 2005).

In some cases guanosine produces its effects by entering cells and interacting with an NGF-dependent protein kinase (Jiang et al., 2006) and under certain circumstances, guanosine acts synergistically with certain growth factors, such as NGF to produce its effects. Guanosine has also been shown to promote the release of adenosine from cells (Ciccarelli et al., 2000); however, most of the effects of guanosine are different from those of adenosine and cannot be explained by adenosine release (Di lorio et al., 2002).

To date the mechanism through which guanosine exerts its biological effect remains unclear. Many effects of extracellular purine nucleosides and nucleotides are mediated through G-Protein Coupled purine receptors—‘purinoceptors’ (Burnstock G., 2007) that have common structural features. Preliminary evidence for the existence of a high-affinity binding site, specific for guanosine in rat brain membranes (Traversa U., et al., 2002; Traversa et al., 2003; Volpini et al., 2011), analogous to the adenine receptor (Wengert M et al., 2007) has been obtained. Accordingly, it is believed that guanosine is responsible for the activation of a number of intracellular signalling pathways. These intracellular signalling pathways, for example, result in the elevation of cAMP in rat brain membranes (Traversa et al., 2003) and in primary stem cells (Su et al., 2013), PI3kinase/Akt/PKB and mitogen-activated protein kinase and ERK1/2 phosphorylation which are characteristic responses of activated G-Protein Coupled Receptors (Di lorio P et al., 2001; Pettifer et al, 2007; Traversa U., et al., 2002; Ballerini et al., 2006; Di lorio et al., 2004; Giuliani et al., 2012). The addition of exogenous guanosine to cultured mouse primary astrocytes also leads to the elevation of intracellular calcium concentrations, although it is unclear whether this is mediated via the putative Guanosine receptor (Chen et al., 2001). Interestingly, the effects of guanosine on the production of trophic factors by astrocytes and the anti-apoptotic effects of guanosine are sensitive to pertussis toxin, an inhibitor of Gi and Go coupled G-protein Receptors (Fields T A and Casey P J, 1997), and are not inhibited by inhibitors of nucleoside or nucleobase transport, which lends support for the hypothesis that guanosine acts extracellularly. Furthermore, rat brain membranes have been shown to have high affinity cell surface binding sites specific for guanosine>>inosine that do not bind adenosine (Traversa U., et al., 2002).

On the basis of pharmacological and molecular cloning studies, the International Union of Pharmacology Committee on Receptor Nomenclature and Drug Classification (NC-IUPHAR) has subdivided purinoceptors into two major classes: adenosine (P1) receptors and nucleotide (P2) receptors (Fredholm et al., 2001; Abbracchio and Burnstock, 1994). Four subtypes of adenosine receptors have been identified: A₁, A₂A, A₂B, and A₃. Each has a unique tissue distribution, signal transduction mechanism, and ligand affinity. All adenosine receptor subtypes are coupled to heterotrimeric G proteins. Activation of A₁ or A₃ subtypes inhibits adenylate cyclase activity, whereas activation of A₂A and A₂B subtypes stimulates adenylate cyclase activity. Additionally, A₁ and A₃ subtypes are coupled to other signal transduction pathways, including phosphoinositol hydrolysis and potassium channels (Ramkuran et al., 1993; Linden, 1991).

In addition to their different effects, these receptor subtypes can also be distinguished by the potency order of a series of agonists and antagonists (Palmer and Stiles, 1995). Adenosine is the preferred endogenous agonist at all adenosine receptors. But the naturally-occurring purine inosine, for which no unique receptor has been identified, binds to, and activates A₃ receptors (Jin et al., 1997; Linden et al., 1985), producing immunomodulatory and neuroprotective effects (Gomez and Sitkovsky, 2003; Hasko et al., 2004). A₃ receptor subtypes exhibit the lowest degree of amino acid sequence identity either with different species homologues (Palmer and Stiles, 1995; Fredholm et al., 2001) or with other adenosine receptor subtypes, resulting in unique pharmacological properties (Linden et al., 1993).

P2 receptors are further divided into P2X ligand-gated ion channels, which are activated solely by ATP, and G-Protein Coupled P2Y receptors which are activated both by extracellular adenine and uracil nucleotides. Eight P2Y receptors (P2Y1, 2, 4, 6, 11, 12, 13, 14) have been cloned from mammalian tissues (Abbracchio 2003, Zhang 2002, North 2002, Fredholm, 1997). P2Y receptor activation stimulates phosphoinositol hydrolysis. Additionally, activation of P2Y12, 13, 14 receptors inhibits adenylyl cyclase whereas P2Y11 activation stimulates this enzyme (von Kugelgen and Wetter, 2000).

P1 and P2Y purinoceptors are integral membrane proteins that belong to the class A, rhodopsin-like, G-Protein Coupled Receptor (GPCR) superfamily. These purinoceptors are predicted to share a conserved molecular architecture consisting of seven hydrophobic transmembrane domains (TMDs), which span the plasma membrane, connected by three intracellular and three extracellular loops (Watson et al., 1994).

It is difficult to extract and crystallise GPCRs. Indeed, only the rhodopsin receptor has been crystallised and studied by X-ray diffraction. However, it has been possible to predict the tertiary structure of other GPCRs based on the atomic co-ordinates of the rhodopsin receptor. Since P1 and P2Y receptors have not been crystallised, an understanding of how purinoceptors bind their cognate ligands is based on modelling studies combined with site-directed mutagenesis. GPCRs have low amino acid sequence homology. However, there are several highly conserved key amino acid residues which may be essential for either the structure or function of the receptors. As in other receptor families, similarity between sequences of the P1 or P2Y receptor family is greatest in the hydrophobic TMDs.

Certain well-conserved amino-acid residues of the P2Y receptor subfamily have been used to identify and clone new P2Y receptors (Chambers et al., 2000; Communi et al., 2001; Joost and Methner et al., 1997; Jiang et al., 1997). In contrast, no orphan receptor related to the P1 receptor subfamily has been identified. However, mutational data have identified some amino acid residues important for ligand binding to adenosine receptors (Fredholm et al., 2001).

This background information is provided to reveal information believed by the applicants to be of possible relevance. No admission is necessarily intended, nor should it be construed, that any of the preceding information constitutes prior art.

SUMMARY

The following presents a simplified summary of the general inventive concepts described herein to provide a basic understanding of some aspects of the invention. This summary is not an extensive overview of the invention. It is not intended to restrict key or critical elements of the invention or to delineate the scope of the invention beyond that which is explicitly or implicitly described by the following description and claims.

Based on the evidence of G-Protein Coupled Receptors specific for adenosine and the suspected existence of a receptor for guanosine as well as the intracellular responses of exogenously added guanosine to tissue cultures, inter alia, an investigation was undertaken to locate motifs in the primary sequence of the TMDs of P1 adenosine receptors, which may be important for the binding of guanosine. Accordingly, adenosine A₃ receptor-like sequences among orphan receptors were searched given that A₃ receptors bind inosine as discussed in more detail below. The sequences of orphan receptors were analyzed to identify similar motifs. Through such studies, G-Protein Coupled Receptor 22 (GPCR22—SEQ. ID NO: 3) was identified as a possible G-Protein Coupled Receptor able to bind guanosine. Surprisingly, further research verified GPCR22 as a novel guanosine binding receptor. Guanosine was shown in further studies, discussed below, to make functional binding to GPCR22 when expressed in cells which do not normally express the GPCR22 receptor. Additionally, Guanosine, binding to GPCR22 was also shown, using biochemical, pharmacological and physiological techniques, to elicit cellular effects in such cells.

It would be desirable to identify a method useful for identifying guanosine analogues which may act as agonists, partial agonists and inverse agonists on a G-Protein Coupled Receptor able to bind guanosine. Furthermore, in some embodiments it would be desirable to provide a means for identifying various cell types expressing a receptor able to bind guanosine.

In one aspect there is provided a transformed cell line expressing a non-endogenous G-Protein Coupled Receptor. The transformed cell line is proliferated from a host cell having been transformed to express a cell-surface G-Protein Coupled Receptor able to bind guanosine and guanosine analogs. In some embodiments, the host cell is transfected with a recombinant cDNA sequence coding for an amino acid sequence of the cell-surface G-Protein Coupled Receptor able to bind guanosine and guanosine analogs. In preferred embodiments, the amino acid sequence corresponds to GPCR22. Furthermore, in some embodiments, the recombinant cDNA sequence comprises SEQ. ID NO: 1 or SEQ. ID NO: 2. In some embodiments, the amino acid sequence comprises SEQ. ID NO: 3. In preferred embodiments, the host cell is a Drosophila Schneider 2 cell or a human astrocytoma 1321N1 cell.

In another aspect, there is provided a method for producing the transformed cell line as defined above. The method comprises transfecting the host cell with an expression vector, where the expression vector comprises a polynucleotide and the polynucleotide comprises a nucleotide sequence encoding for a polypeptide comprising the amino acid sequence of SEQ. ID NO. 3.

In yet another aspect, there is provided a method for identifying a compound bindable to a selective guanosine responsive G-Protein Coupled Receptor. The method comprises contacting one or more candidate compounds with a host cell transformed to express a receptor comprising an amino acid sequence comprising SEQ. ID NO: 3; and measuring the ability of the one or more candidate compounds to stimulate or inhibit a cellular function associated with said receptor. In some embodiments, the amino acid sequence is encoded by DNA comprising SEQ. ID NO: 1 or SEQ. ID NO: 2. Furthermore, in some embodiments, the cellular function evaluation comprises measuring apoptosis regulation, intracellular calcium mobilization, intracellular protein phosphorylation or a second messenger intracellular pathway activation. In some embodiments, the host cell is a Drosophila Schneider 2 cell or a human astrocytoma 1321N1 cell. Furthermore, in some embodiments, the one or more candidate compounds may be an agonist, a partial agonist or an inverse agonist of the receptor.

In another aspect, there is provided a method for transforming a host cell to express a guanosine bindable G-Protein Coupled Receptor. The method comprises transfecting a host cell with an expression vector, where the expression vector comprises a polynucleotide sequence comprising SEQ. ID NO: 1 or SEQ. ID NO: 2, encoding for a polypeptide comprising an amino acid sequence comprising SEQ. ID NO: 3; and wherein the host cell under the appropriate culture conditions, produces a polypeptide comprising the amino acid sequence of SEQ. ID NO: 3. In preferred embodiments, the polypeptide comprising SEQ. ID NO: 3 corresponds to GPCR22 and is expressed at the cell surface. In preferred embodiments, the host cell is a Drosophila Schneider 2 cell or a human astrocytoma 1321N1 cell.

In yet another aspect, there is provided a G-Protein Coupled Receptor capable of binding guanosine or analogs thereof. In some embodiments the G-Protein Coupled Receptor has an amino acid sequence having at least 70% homology to SEQ. ID NO: 3. In some embodiments the G-Protein Coupled Receptor has an amino acid sequence having at least 80% homology to SEQ. ID NO: 3. In some embodiments the G-Protein Coupled Receptor has an amino acid sequence having at least 90% homology to SEQ. ID NO: 3. In some embodiments the G-Protein Coupled Receptor has an amino acid sequence having at least 95% homology to SEQ. ID NO: 3. In some embodiments, the G-Protein Coupled Receptor capable of binding guanosine or analogs thereof, has an amino acid sequence corresponding to SEQ. ID NO: 3.

In another aspect, there is provided a method for identifying a cell having a G-Protein Coupled Receptor able to bind guanosine or analogues thereof. The method comprises extracting DNA from a population of subject cells, executing a polymerase chain reaction (PCR) technique on said DNA extracted from said population of subject cells using a forward primer corresponding to SEQ ID NO: 5. and a reverse primer corresponding to SEQ. ID NO: 6 and analyzing the PCR product resultant therefrom.

In still yet another aspect, there is provided a transformed cell line expressing a non-endogenous G-Protein Coupled Receptor capable of binding guanosine or analogues thereof wherein the non-endogenous G-Protein Coupled Receptor has a guanosine or analogue thereof binding domain located in transmembrane domain 6, where the binding domain comprises SEQ. ID NO: 7 or SEQ ID NO: 8. In preferred embodiments, the transformed cell line is from a Drosophila Schneider 2 cell or a human astrocytoma 1321N1 cell transfected to express GPCR22.

Other aims, objects, advantages and features of the invention will become more apparent upon reading of the following non-restrictive description of specific embodiments thereof, given by way of example only with reference to the accompanying drawings.

BRIEF DESCRIPTION OF THE FIGURES

In order that the invention may be better understood, exemplary embodiments will now be described by way of example only, with references to the accompanying drawings, wherein:

FIG. 1 is a photograph of a gel electrophoresis showing the expression of GPCR22 (G1) determined by real-time PCR in cultured rat astrocytes;

FIG. 2a is a photograph of a gel electrophoresis showing the silencing of GPCR22 (G1) by siRNA determined by real-time PCR in cultured rat astrocytes compared to cultured rat astrocytes not treated with siRNA for GPCR22;

FIG. 2b is a photograph of a Western Blot showing the silencing of GPCR22 protein in cultured rat astrocytes by siRNA;

FIG. 3 is a photograph of a gel electrophoresis of Plasma DNA indicating positive cloning for GPCR22;

FIG. 4 is a photograph of a gel electrophoresis showing the expression of GPCR22 determined by real-time PCR from rat striatum, non-transfected normal Drosophila Schneider 2 cells and GPCR22 transfected Drosophila Schneider 2 cells;

FIG. 5 is a photograph of a gel electrophoresis showing that 1321N1 human astrocytoma cells do not express GPCR22 (G1) as determined by real-time PCR;

FIG. 6a is a photograph of a gel electrophoresis showing the transfection of GPCR22 (G1) DNA into 1321N1 human astrocytoma cells determined by real-time PCR;

FIG. 6b is a photograph of a Western Blot showing the expression of GPCR22 protein following GPCR22 (G1) DNA transfection into 1321N1 human astrocytoma cells;

FIG. 7a is a photograph of a Western Blot showing Erk 1/2 phosphorylation by guanosine in cultured rat astrocytes and cultured rat astrocytes treated with siRNA for GPCR22 and ns-siRNA;

FIG. 7b is a photograph of a Western Blot showing Akt phosphorylation by guanosine in cultured rat astrocytes and cultured rat astrocytes treated with siRNA for GPCR22 and ns-siRNA;

FIG. 7c is a photograph of a Western Blot showing Erk 1/2 phosphorylation by guanosine in 1321N1 human astrocytoma cells and 1321N1 human astrocytoma cells transfected with GPCR22 DNA;

FIG. 7d is a photograph of a Western Blot showing Akt phosphorylation by guanosine in 1321N1 human astrocytoma cells and 1321N1 human astrocytoma cells transfected with GPCR22 DNA;

FIG. 7e is a graph showing the effect of guanosine on increasing intracellular cAMP concentrations in 1321N1 cells transfected with GPCR22 (G1) receptor DNA in the absence and in the presence of, 3 μM forskolin and 3 μM forskolin plus pertussis toxin (200 ng/ml, 16 h);

FIG. 8 shows the sequence confirmation results of GPCR22-pMT-GPCR22-Forward GPCR22 transfection in Drosophila Schneider 2 transformed cells;

FIG. 9 shows the sequence confirmation results of GPCR22-pMT-GPCR22-Reverse GPCR22 transfection in Drosophila Schneider 2 transformed cells;

FIG. 10 is a photograph of a Western Blot showing GPCR22 (G1) protein expression in transfected Drosophila Schneider 2 cells;

FIGS. 11 a to d are graphs of flow cytometry data showing the anti-apoptotic effects of guanosine on GPCR22 transformed Drosophila Schneider 2 cells in relation to Caspase-3 activity;

FIG. 12a is a fluorescence image showing the effect of guanosine on the level of intracellular Ca²⁺ in non-GPCR22-transfected Drosophila Schneider 2 cells;

FIG. 12b is a fluorescence image showing the effect of guanosine on the level of intracellular Ca²⁺ in GPCR22-transfected Drosophila Schneider 2 cells;

FIG. 12c is a graph showing the effect of guanosine on intracellular Ca²⁺ concentration in GPCR22-transfected Drosophila Schneider 2 cells;

FIG. 12d is a graph showing the effect of guanosine on intracellular Ca²⁺ concentration in non-GPCR22-transfected Drosophila Schneider 2 cells;

FIGS. 13 a to d are fluorescence images showing the effect of guanosine on the level of intracellular Ca²⁺ in GPCR22-transfected Drosophila Schneider 2 cells over a time course;

FIG. 13e is a graph showing an intracellular Ca²⁺ response to guanosine in GPCR22-transfected Drosophila Schneider 2 cells;

FIG. 13f is a graph showing high dose (25 μM-400 μM) guanosine-induced intracellular Ca²⁺ response in GPCR22-transfected Drosophila Schneider 2 cells;

FIG. 13g is a graph showing a time course of low dose (0.1 μM-10 μM) guanosine-induced intracellular Ca²⁺ response in GPCR22-transfected Drosophila Schneider 2 cells;

FIG. 14 is a Saturation Binding curve graph of guanosine to GPCR22 receptors; and

FIG. 15 is a graph showing GPCR22/guanosine mediated intracellular Ca2+ increase in GPCR22-transfected Drosophila Schneider 2 cells.

BRIEF DESCRIPTION OF THE SEQUENCES

SEQ. ID NO: 1 is an exemplary cDNA polynucleotide sequence having 100% homology to Rat GPCR22 and 97% homology to mouse GPCR22 using the exemplary forward primer of SEQ. ID NO: 5 of the instant disclosure;

SEQ. ID NO: 2 is a cDNA polynucleotide sequence having 100% homology to Rat GPCR22 and 97% homology to mouse GPCR22 using the exemplary reverse primer of SEQ. ID NO: 6 of the instant disclosure;

SEQ. ID NO: 3 is an exemplary amino acid polypeptide sequence corresponding to GPCR22 of the instant disclosure;

SEQ. ID NO: 4 is an exemplary mRNA polynucleotide sequence corresponding to a mouse GPCR22 of the instant disclosure;

SEQ. ID NO: 5 is oligonucleotide sequence corresponding to an exemplary forward primer for GPCR22 of the instant disclosure;

SEQ. ID NO: 6 is oligonucleotide sequence corresponding to an exemplary reverse primer for GPCR22 of the instant disclosure; and

SEQ. ID NO: 7 is a polypeptide sequence of an exemplary GPCR22 transmembrane 6 binding domain of the instant disclosure; and

SEQ. ID NO: 8 is a polypeptide sequence of an exemplary GPCR22 transmembrane 6 binding domain of the instant disclosure.

DETAILED DESCRIPTION

With reference to the disclosure herein and the appended figures, cell lines transformed to express GPCR22 and a method for identifying guanosine analogues which may be agonists, partial agonists and inverse agonists of GPCR22 are described in accordance with various embodiments of the invention.

Example 1: Identification of the G1 Receptor Using Bioinformatic Approaches

Based on the pharmacological and transductional evidence supporting the existence of the putative G1 receptor, preliminary structural data using bioinformatic approaches was used to identify possible orphan G-Protein Coupled Receptors capable of binding guanosine. Using DNA and Protein databanks, the sequence motifs of the 7 transmembrane segments (TMs) for the adenosine A₁, A₃, A_(2a) and A_(2b) receptors, which are highly conserved among these receptor subtypes were used to identify possible candidates for guanosine bindable orphan G-Protein Coupled Receptors. Inosine, a purine similar structurally to guanosine, is known to interact with the adenosine A₃ receptors, as well as having been shown to bind to the putative G1 binding site in rat brain. Therefore, the sequence for the TMs 3, 5, 6 and 7 of the human adenosine A₃ receptors was selected, which constitutes the hydrophobic binding pocket for both, agonists and antagonists (Moro et al., 2005), and screened against the sequences of some of the orphan G-Protein Coupled Receptors (GPCRs) in the databanks. Based on this sequence homology to the human adenosine A₃ receptor several orphan GPCRs with potential G1 (guanosine) receptor activity were identified.

Many of the amino acid residues important for ligand binding to ATP or adenosine receptors are located in the sixth TMD (Fredholm et al., 2001). Accordingly, a multiple sequence alignment (Clustal-W program, blosum matrix) and Sequence motif search (http://expasy.org) was used to develop novel patterns within the sixth TMD characteristic of P2Y and P1 receptors.

It was noted that the local sequence: hhx[CS][FY]hPhHhx[RK] is shared among all P2Y sequences reported at SwissProt and GeneBank databases. This consensus pattern, when scanned against sequence databases, matched only with proteins belonging to P2Y class. However, this pattern also contains residues which are maintained in all metabotropic purinoceptors. In particular at 254, 255, 259 and 261 positions (referring to the numbering of the human P2Y2 receptor) a hydrophobic residue (h) is strictly conserved in all P1 and P2 receptors. The role of these hydrophobic residues is unknown. A Pro residue (at position 261) is also strictly maintained in all metabotropic purinoceptors. This represents one of the most conserved amino acid residues in the GPCR superfamily. Analysis of the crystal structure of the rodhopsin receptor and mutagenesis studies indicates that the corresponding Pro267 plays a critical role in the overall protein conformation (Okada et al., TiBS 2001; Ridge et al., 1999). The function of the [CS] residue, strictly maintained at position 257 in all P2Y and P1 receptors, has never been investigated.

Mutagenesis studies indicate that single substitution of the conserved His-262 and Arg-265 with leucine decreased the potency but not the efficacy of ATP and UTP on the P2Y2 receptor, suggesting that these amino acid residues are mainly involved in the ligand binding (Erb et al., 1995). Molecular modelling studies also indicate that His-262 and Arg-265 interact with negatively charged phosphate residues of ATP (Erb et al., 1995). Arg-265 is always present in P2Y nucleotide receptors except for P2Y1 and P2Y6 in which a Lys residue occurs in an analogous position. Thus a positive charged residue at position 265 seems to be needed for nucleotide binding (Erb et al., 1995; von Kugelgen and Wetter, 2000).

In the TM6 domain, the consensus pattern of P1 receptors is clearly distinct from that of the P2Y. In particular the A₁, A₂A and A₂B subtypes are generally characterised by the conserved local motif hhx[CS]WhPhHxxNxhTxF, whereas A₃ receptors contain a different consensus pattern hhx[CS]WhPh[CS]hxNxhxxF. The sequence alignment showed that His-262 residue is strictly maintained in P2Y as well as in all A₁, A₂a and A₂b receptor subtypes, but not in A₃ receptor sequences. Several mutagenesis studies have demonstrated that in A₁, A₂a and A₂b subtypes this highly conserved His is involved in ligand binding (Olah et al., 1992; Kim et al., 1994). In the TM6 domain of all A₃ adenosine receptors, the His-262 is always replaced by a Ser residue. Mutagenesis studies indicate that Ser-247 of human A₃ receptors is not involved in agonist binding but, rather, in that of antagonists (Gao et al., 2002). Although adenosine is the main endogenous agonist at A₃ receptors, inosine can also activate them (Jin et al., 1997; Linden et al., 1995; Fredholm et al., 2002), as noted above. The presence of a Ser, instead of His, residue is peculiar to A₃ receptors. Whether this His plays a role in inosine binding is unknown.

The alignment also revealed that the Lys/Arg residue (265 in P2Y2), involved in the interaction with charged phosphate residues of ATP and present in all P2Y receptors (Erb et al., 1997), is replaced by an Asn residue in an analogous position (250 A₃ and 253 A₂A) in all P1 subtypes. Mutational studies indicate that this conserved Asn is involved either in receptor-ligand recognition or in maintaining receptor structure (Kim et al., 1995; Gao et al., 2002). In contrast to P2Y receptors, a Trp residue (Trp-243 in the human A₃ receptor) is rigorously maintained in all P1 sequences. This residue is appears to be needed for activation of the A₃ receptor but not for agonist binding (Gao et al., 2002), since substitution of the Trp-243 by a Phe residue impairs the ability of agonists to activate PLC (Gao et al., 2002). A Thr residue (Thr-257 in human A₁) is highly conserved in A₁, A₂a and A₂b subtypes, distinguishing A₁ and A₂ from A₃ receptor sequences. The consensus residue Phe-262 (in human A₁) is unique to the P1 class. No characteristic residue is found at a homologous position in P2Y receptors.

The identification of a specific pattern for the A₃ s has been shown to be a good approach to predict ligands for additional A₃-related orphan receptor. This pattern was built so as to contain residues that are of the P1 receptor subfamily, especially those that can form plausible intermolecular interaction with the ligand class (inosine). Among orphan GPCRs, only one met the above-note characteristics as discussed below.

Therefore, a consensus pattern of hhx[CS]WxPh[CS]hxNxhxxF, was defined that contained residues specific for the A₃ subtype of P1 receptors, for which inosine as well as adenosine is an agonist. When scanned against sequence databases the consensus pattern matched only with A₃ receptor subtypes. However when the consensus sequence was shortened to hhx[CS]WxPh[CS]hxN, the pattern also matched the orphan G-Protein Coupled Receptor 22 (GPCR22) from human, rat and mouse.

By comparing the amino acid sequences of the A₃ receptors against that of GPCR22, it was surprisingly discovered that the overall percentage of identity between adenosine A₃ receptors and GPCR22 is low, being about 13%. However, if only TM6 is considered, the percentage of identity rises to 30%. Therefore, as result of the above analysis, it was determined that there may be a binding domain in TM6 of GPRC22 for guanosine represented by hhx[CS]WxPh[CS]hxN. For example, using the A₃ receptor amino acid alignment as a reference, the binding domain may be located beginning at TM6 amino acid residue 239, preceded by two hydrophobic residues at positions 239 and 240, and additional hydrophobic residues at locations 246 and 248. Accordingly, the binding domain may be as follows, where h denotes hydrophobic residues and x denotes unknown amino acid residues: h-239, h-240, x-241, Ser-242, Trp-243, x-244, Pro-245, h-246, Ser-247, h-248, x-249, Asn-250 or h-239, h-240, x-241, Cys-242, Trp-243, x-244, Pro-245, h-246, Cys-247, h-248, x-249, Asn-250, noted below as SEQ. ID NO: 7 and SEQ. ID NO: 8, respectively.

Notably, in addition to strictly conserved residues typical of the P1 receptors, GPCR22 shares a Ser residue analogous to Ser-247 of the human A₃ receptor. GPCR22 shares a higher sequence identity with the cholecystokinin-B receptor (34%) (O'Dowd et al., 1997) than with the A₃ receptor. Nevertheless, GPCR22 (SEQ. ID NO: 3) shares with A₃ receptors residues in TM6 that are specific for P1 receptor subfamily, and which are believed to be likely important in purine nucleoside ligand binding.

These data indicate that GPCR22 may have substrate binding characteristics related to an A₃ receptor. Although adenine nucleotides and adenosine are the prototypical purinergic signalling molecules, non-adenine-based purines, including guanosine and inosine, have recently been shown to have important neuromodulatory roles (Soares et al., 2004; Gomez and Sitkovsky, 2003). Moreover, as noted above, a receptor-like cell surface binding site for guanosine has been identified (Traversa et al., 2002; Traversa et al., 2003). Therefore, it was investigated as to whether the orphan receptor GPCR22 is a novel nucleoside receptor.

Based on the above-noted analysis, GPCR22 was selected as a potential candidate for a G-Protein Coupled Receptor capable of binding guanosine, also referred to herein as the G1 receptor, and producing cellular effects.

Example 2: Inhibition of GPCR22 by siRNA in Primary Astrocytes

GPCR22 Expressed in Cultured Rat Astrocytes:

With reference to FIG. 1, RT-PCR experiments showed that GPCR22, the G1 receptor, as also referred to herein, is expressed in cultured rat astrocytes. The primers used for the RT-PCR experiments were GPCR22 forward: CTC ATC TGC TGT TTC CAC GA (SEQ. ID NO: 5) and GPCR22 reverse CGG ATG TTA AGA GCC TGG AG (SEQ. ID NO: 6).

siRNA for GPCR22 Experiments on Cultured Rat Astrocytes:

Transient transfection of siRNAs for the rGPCR22 gene on rat cultured astrocytes and cell extracts were assayed for gene silencing 24 h after transfection was carried out. siRNA duplex specific for the rGPCR22 receptor were designed and chemically synthesized (http://www.Dharmacon.com), as well as their non specific control (NSC). Transfection of siRNAs for targeting endogenous genes was carried out using Oligofectamine (Invitrogen, Life Technologies) according to the manufacturer's instruction. Briefly, astrocytes at 60-70% confluence were cultured for 1 day in culture medium without antibiotics. 10 □l siRNA (20 □M) (Dharmacon research, Inc.) were diluted in 175 □l optimem for 5 min at room temperature. In the meantime 3 □l oligofectamine was mixed in 15 □l optimem for 5 min. RNA interference was performed by mixing diluted oligofectamine and siRNA for 30 min at room temperature and was then added to the cells. The same scheme was performed on other samples using a siRNA-scrambled (NSP=non specific control). Cells were incubated at 37° C. for 24 hours. Twenty-four hours after transfection, the cells were lysed and assayed for gene silencing. The effect of GPCR22 silencing on MAPK and AKT phosphorylation, and cAMP assay was analysed.

Using siRNA for GPCR22 in cultured rat astrocytes, the expression of GPCR22 (G1) was shown to be abolished by RT-PCR, as shown in FIG. 2a . FIG. 2a shows the results of RT-PCR for the GPCR22 DNA (G1) in cultured rat astrocytes and cultured rat astrocytes treated with siRNA for GPCR22 (G1-siRNA). Additionally, through Western Blot analysis (FIG. 2b ) using a rabbit polyclonal anti-GPCR22 antibody (NovateinBio, SH-A12465, MA, USA) it was shown that the GPCR22 protein expression in cultured rat astrocytes was inhibited by siRNA. Furthermore, in astrocytes, inhibition of GPCR22 by siRNA was shown to abolish both guanosine binding and activation of intracellular signaling by guanosine (data not shown).

Example 3: Transfection of hGPCR22 in 1321N1 Human Astrocytoma Cells

GPCR22 is not Expressed in 1321N1 Human Astrocytoma Cells:

With reference to FIG. 5, RT-PCR experiments showed that GPCR22 (G1) is not expressed in 1321N1 human astrocytoma cells. The primers used for the RT-PCR experiments were GPCR22 forward: CTC ATC TGC TGT TTC CAC GA (SEQ. ID NO: 5) and GPCR22 reverse CGG ATG TTA AGA GCC TGG AG (SEQ. ID NO: 6).

Transient Transfection of hGPCR22 in 1321N1:

A full length cDNA clone of human GPCR22 was provided by Origene Technologies. Transient expression in the 1321N1 cell line was performed using a pCMV expression vector. cDNA fragments present in an expression vector (pCMV) is located downstream of a transcriptional promoter capable of driving heterologous gene expression in a variety of mammalian cells. 1321N1 cell lines were transiently transfected with hGPCR22 cloned into pCMV expression vectors (Invitrogen). DNA transfection was performed by lipofection using Lipofectamine (Life Technologies). Twenty-four hours after transfection, the cells were lysed and assayed. RT-PCR analysis using GPCR22 forward: CTC ATC TGC TGT TTC CAC GA (SEQ. ID NO: 5) and GPCR22 reverse CGG ATG TTA AGA GCC TGG AG (SEQ. ID NO: 6), was used to confirm the transfection of GPCR22 (G1) (labelled “1321N1 G1-pCMV Trans”) into 1321N1 cells as shown in FIG. 6a and evidenced by the band at 411 bp. Furthermore, the expression of GPCR22 (labelled “1321N1 G1-pCMV Trans”) in 1321N1 cells as compared to non-G1 transfected cells (labelled “1321N1”) was confirmed by Western Blot analysis using a rabbit polyclonal anti-GPCR22 antibody (NovateinBio, SH-A12465, MA, USA), as shown in FIG. 6 b.

Stable Transfection of hGPCR22 in 1321N1:

It was determined from the above-noted assays that the pCMV vector could not be used for stable transfection. Therefore hGPCR22 was cloned into a pCDNA3.1 vector. The cloning procedures were performed by mean of total RNA extraction from the cells expressing high levels of the receptor. Subsequently a retro-transcription reaction was carried out according to the manufacturer's instructions. Specific oligonucleotide PCR primers external to the putative open reading frame (ORF) of the human receptor sequence were designed for PCR confirmation of stable transfection. PCR reactions to ascertain stable transfection were performed in MgCL₂ (1.5 mM), dNTP (1 mM), oligonucleotides (100 pmol), Taq Gold (0.5 U, PerkinElmer), with an annealing temperature of 55° C. The PCR product was ligated to an expression vector by utilizing the pCDNA3.1N5-His©TOPO®TA Expression kit (Invitrogen, Italy) according to the manufacturer's instructions. Cloned sequences were verified by sequencing.

1321N1 cell lines were stably transfected with GPCR22 cloned in pCDNA3.1 expression vectors (Invitrogen). 1321N1 cells were seeded at 150,000 cells/dish. Transfections were performed 24 hours after seeding with 2 ug DNA and 4 ul lipofectamine (Life Technologies). DNA Selection was performed using 600 ug/ml geneticin. After selection individual colonies were maintained in 300 ug/ml geneticin.

Example 4: GPCR22 Mediated Intracellular Effects

Phosphorylation of Erk 1/2 and Akt:

FIGS. 7a and 7b , respectively, show that the phosphorylation of Erk 1/2 and Akt by guanosine (300 μM) is inhibited in cultured rat brain astrocytes treated with si-RNA for GPCR22; thus lending support that GPCR22 is indeed a G-Protein Coupled Receptor for guanosine, and analogues thereof. Similarly, as shown FIGS. 7c and 7d , respectively, in 1321N1 cells transfected with GPCR22 DNA (labelled “G1-pCMV Trans) so as to express the GPCR22 receptor, guanosine (300 μM) treatment of the cells resulted in phosphorylation of both Erk 1/2 and Akt compared to non-GPCR22-transfected 1321N1 cells (labelled “Non-Trans”) which do not endogenously express GPCR22.

Intracellular cAMP Increase by Guanosine in 1321N1 Cells Transfected with GPCR22:

FIG. 7e shows the effects of increasing concentrations of exogenously applied guanosine on 1321N1 cell line transfected with GPCR22 (G1) receptor in the absence and in the presence of PTX (200 ng/ml, 16 h). Accordingly, it is shown that guanosine acts to produce cellular effects through GPCR22 and increase intracellular cAMP levels.

Example 5: Transfection of GPCR22 in Drosophila Schneider 2 (S2) Cells

A Full Length cDNA Clone of Rat GPCR22:

RNA from Rat striatum area was extracted using the Trizol method and then purified with Ambion RNA mini kit according to the manufacture instruction (Ambion RNA mini Kit, Cat: 12183020). cDNA of rGPCR22 was synthesized using Quanta Biosciences 95049-100 (qScript Flex cDNA synthesis kit), PCR polymerase (Invitrogen Platinum@ Taq DAN polymerase High Fiidelity) and PCR water (GIBCO 10977 Ultrapure distilled water) following the manufacture's instructions. GPCR22 forward: CTC ATC TGC TGT TTC CAC GA (SEQ. ID NO: 5) and GPCR22 reverse CGG ATG TTA AGA GCC TGG AG (SEQ. ID NO: 6) were used. GPCR22 PCR product was tested by running 1% agarose gel following the instructions (Invitrogen). Gene Ruler 1 KB ladder was purchased from Thermo Scientific (SM3011). 5× loading buffer was used to load PCR product, and the gel was run at 100V until the front of the ladder reached the bottom of the gel. The results were detected under UV light. After confirmation of GPCR22 size with agarose gel, the correct band was cut and PCR product (cDNA of GPCR22 whole sequence) was extracted from the gel using Qiaex II Gel extraction kit (Qiagen 20021) as instructed by the manufacture. The extracted GPCR22 whole sequence was sent for sequencing to confirm the identity (Mobix service at McMaster University).

Preparation of GPCR22/pMTN5/HisA Plasmid DNA for Transfection:

The restriction enzyme sequences were added to the primers described as follows. Primers for GPCR22: Kpn I was added to the forward sequence and Apa I to the reverse sequence for whole cloned sequence of GPCR22. Extra base was also added for easier digestion. Restriction enzyme recognition sequence for the restriction enzymes used is underlined as follows—GPCR22 forward: Kpn I 5′-TAG GGT ACC ATG TCA GAA TTG TCA AT-3′; GPCR22 reverse: Apa I 5′-CTA GGG CCC CTA GTC TGT GAC AAC CT-3′. pMT-V5-HisA, pMT-V5-His-Lacz and pCoHygro vectors were used. The inducible expression vector pMT-V5-HisA has a metallothionein (MT) promoter, and was induced by the addition of copper sulfate to the culture medium. It was stored in DH5α E. Coli. in a −80° C. freezer. Vector extraction was done using Qiagen Qia prep-SPIN minikit (Qiagen 27104) or Qiagen Hispeed Plasmid Max kit (Cat: 12662) according to the instructions from the manufacture. Using the following primer to clone PMT and COPIA sequences from the extracted vector DNA, and gel extracted PCR product were sent for sequencing to confirm the pMT vector (Mobix service at McMaster University). Primer for pMT and COPIA: PMT forward: CAT CTC AGT GCA ACT AAA; Copia forward: TGT TGG AAT ATA CTA TTC AAC CTA CAA.

The GPCR22 PCR products or the pMT vector plasmid DNA extraction was prepared through the sequential digestion, first using the restriction enzyme Apa I (Fermentas, Cat# ER1415). The digested products were then separated with electrophoresis and extracted with Qiaex II Gel extraction kit (Qiagen 20021). The extracted product was then subjected to a second digestion with the restriction enzyme Kpn I (Fermentas, Cat# ER0521), and then separated using gel electrophoresis and extracted with Qiaex II Gel extraction kit for further ligation. GPCR22 PCR product was digested at 37° C. for 2.5 hr, and the vectors were digested at 37° C. for 1.5 hr. Both of the reactions were deactivated at 60° C. for 20 min after the digestion.

To calculate the amount of DNA required, 1:1 ratio (pMT/V5/HisA plasmid DNA: GPCR22 DNA), the amount was calculated according to the following formula: The amount of GPCR22 DNA=bp GPCR22 PCR product×the amount of Vector/bp of vector. Ligation was performed at 14° C. for overnight. Transformation of the ligated mix was done using one-short Top10 competitive E. Coli (Invitrogen, Cat#04040-03) following the manufacture's instruction. Clones were picked from LB plates and cultured separately at 250 rpm, 37° C., LB medium with 100 μg/ml Amp. Plasma DNA was extracted from clones and double digestion was performed with Apa I and Kpn I. After digestion, an electrophoretic gel was run to separate the DNA. The band size and number of bands was judged to foretell whether positive clones had been obtained, as shown in FIG. 3. The potential positive clones were sent for sequencing for confirmation. Once the positive E. Coli clones were confirmed, the culture was continued until a sufficient amount of GPCR22/pMTN5/HisA plasmid DNA for future transfection was obtained.

Transfection of Clone-Recombinant GPCR22 DNA to Drosophila Schneider 2 Cells (S2 Cells):

A calcium method was used for GPCR22 transfection into Drosophila Schneider 2 cells (S2) according to the manufacture's instruction (CalPhos Mammalian Transfection kit, Clontech, Cat No: 631312). Briefly, the Drosophila Schneider 2 cell line (also referred to herein as S2 cells) was purchased from Invitrogen (Cat: R690-07). Cells were cultured, passaged and stored according to the manufacture instruction. S2 cells were maintained at 25-28° C. in Schneider's Drosophila medium (GIBCO) supplemented with 10% heat-inactivated fetal calf serum, penicillin and streptomycin. 1.5×10⁶ S2 cells per well were seeded with Drosophila Schneider 2 cell medium (S2 medium) and cultured for a day before transfection. Then, transfection was performed following the manufacture's recommended procedure. Following 24-hour culture, the S2 cells were collected into 1.5 ml eppendorf tube and labeled properly. The cells were then centrifuged at 3000 rpm for 2 min. in an eppendorf tube. The supernatant was re-suspended in 1 ml of S2 medium with 5 ml of 100 mM CuSO₄ solution (final concentration is 500 mM), then transferred one by one to new 12 well plate and incubated for 2 days.

Example 6: RT-PCR to Determine the Expression of GPCR22 from the Transfected S2 Cells

For real-time PCR analysis total RNA was purified from S2 cells using Trizol (Invitrogen) according to the manufacturer's instructions and incubated with DNase. cDNA was prepared from 5 μg purified RNA using oligonucleotide dT primers. Real-time PCR was performed in an Eppendorf realplex2 PCR machine using SyBr green as a detection reagent. The following primers were used to detect the respective transcripts: Forward Primer (SEQ. ID NO: 5) for GPCR22, 2 μl; Reverse primer (SEQ. ID NO: 6) for GPCR22: 2 μl. Rat cDNA was used as positive control. FIG. 4 shows the PCR testing results that DNA for GPCR22 was successfully transfected into Drosophila Schneider 2 cells.

Example 7: Clone of Recombinated GPCR22 for Transfection

Sequences of Cloned GPCR22:

According to the agarose gel image of FIG. 4, the major band cloned (labeled “Trans-S2) from rat tissue is close to 1.5 KB. This band was cut and DNA was extracted for further sequencing confirmation. The sequencing results, using the forward primer of SEQ. ID NO: 5 and the reverse primer of SEQ. ID NO: 6, to obtain SEQ. ID NO: 1 and SEQ. ID NO: 2, showed that the GPCR22 (Trans-S2 band) cloned from rat stratum is 100% homology to rat GPCRC22 and 97% and 96% to mouse GPCR22 (SEQ. ID NO: 4).

Confirmation of Vector:

Sequence analysis (using Pubmed blast and align function) of vector showed that it is identical to the theoretical sequence for GPCR22.

Electrophoresis Identification of Positive Clone:

DNA was extracted from 8 E. Coli clones and double digested with Apa I and Kpn I. Both the undigested DNA and cut DNA samples were loaded for electrophoresis. Judging from the image electrophoresis image (FIG. 3), 6 out of 8 clones were positive for GPCR22. Samples from those positive DNA was sent for further sequencing confirmation.

Sequencing Confirmation of the Positive Clone:

The sequencing result showed that there were some “failed sequence reaction” identified as “N”, as shown FIG. 8 at both ends of GPCR22-pMT-GPCR22-Forward. Therefore, the data in the middle (underlined sequence, 894 letters, in FIG. 8) was used to do further analysis (to blast in NCBI website) and the result are reported as following: features in this part of subject sequence: component of oligomeric golgi complex 5; G protein-coupled receptor 22; Score=1596 bits (864), Expect=0.0; Identities=869/871 (99%), Gaps=2/871 (0%); Strand=Plus/Minus. Similarly, the sequencing result showed that there were some “failed sequence reaction” identified as “N”, as shown FIG. 9 at both ends of GPCR22-pMT-GPCR22-Reverse. Therefore, the data in the middle (underlined sequence, 871 letters, in FIG. 9) was used to do further analysis. Features in this part of subject sequence: component of oligomeric golgi complex 5; G protein-coupled receptor 22; Score=1578 bits (854), Expect=0.0; Identities=865/871 (99%), Gaps=1/871 (0%); Strand=Plus/Minus.

Example 8: Confirmation of Successful Transfection of Cloned GPCR22 into S2 Cells

Expression of GPCR22 from Transfected S2 Cells Determined by RT-PCR:

FIG. 4 (noted above), shows the expression of GPCR22 determined by real-time PCR from rat striatum (band labeled “Rat), non-transfected normal S2 cells (band labeled “Non-transS2) and GPCR22 transfected S2 (band labeled “Trans-S2), from left to right, respectively, using Forward Primer/SEC). ID NO: 5) for GPCR22, and Reverse primer/SEQ. ID NO: 6) for GPCR22. This data indicates recombinated GPCR22 cDNA was successfully transfected into the S2 cells, while the non-transfected S2 cells did not express any detectable amount of GPCR22.

Example 9: Expression of GPCR22 Protein from Transfected S2 Cells Determined by Western Blotting

Western Blotting and Protein Quantification:

S2 cells were harvested by centrifugation at 1000 g for 3 minutes and lysed on ice for 10 minutes in lysis buffer (Thermofisher with protease inhibiter added, M-PER® Mammalian Protein Extraction Reagent, Thermo Scientific cat#78503; Halt™ Protease and Phosphatase Inhibitor Cocktail, thermo cat#78440). Lysate was spun for 10 minutes at maximum speed, and the supernatant was added to sample loading buffer. Samples were separated by SDS-PAGE and analyzed by western blotting (Rathbone et al., 2011; Connell et al., 2013). Briefly, a rabbit polyclonal anti-GPCR22 antibody (NovateinBio, SH-A12465, MA, USA) was incubated over night at 1:1200 in 1.5% BSA in 1×TBST and a secondary anti-rabbit anti body 1:1000 in 1.5% BSA in 1×TBST was incubated for 1 hr 30 min. Bands were visualized using enhanced chemiluminescence (Amersham Biosciences, Piscataway, N.J.), and quantified on a Kodak Image Station 440CF (New Haven, Conn., USA). Antigens of interest were normalized to anti-GAPDH measured in the same sample.

Western blot technique and analysis using antibody against GPCR22 receptor showed GPCR22 protein expression in S2 cells following transfection indicating that the GPCR22 receptor DNA was successfully transfected into S2 cells and the encoded protein expressed. FIG. 10 shows the results of the Western blotting.

Example 10: Flow Cytometry Experiments

In order to determine whether guanosine produced any anti-apoptotic effects through a GPCR22-mediated mechanism, the effect of guanosine on apoptosis in GPCR22-transfected S2 cells was measured using flow cytometry techniques. Briefly, S2 cells were maintained in Schneider's Drosophila medium (GIBCO) supplemented with 10% heat-inactivated fetal calf serum, penicillin and streptomycin. For induction of apoptosis both receptor-transfected and non-transfected S2 cells were incubated in 1 μM actinomycin D (Sigma) for 6 hours at 25° C. Prior to the induction of apoptosis, to the S2 culture medium were either added 100 μM guanosine or the same amount of vehicle. After a 48 hr incubation with guanosine or vehicle, the cells were fixed with 4% PFA for fluorescent-immunostaining. The primary antibody Caspase-3 (10 μg/ml; R&D systems AF835) was incubated at room temperature for 1.5 hr and the secondary antibody (donkey anti rabbit Alexa488 (1:1800) was incubated at room temperature for 1 hr. After rinsing with PBS cells were re-suspend with “PBS+0.5% BSA” solution for flow cytometry reading using a 8 colour, 2 laser (488 nm, 633 nm, 405 nm) FACS (Canto) machine.

Effect of Guanosine Protecting Cells from Actinomycine-Induced Apoptosis is Regulated by GPCR22:

As shown in FIGS. 11 a to d, guanosine protected transfected S2 cells from apoptotic cell death when it was given to the cells before adding actinomycine into the medium, but had no effect on the normal non-transfected S2 cells, thus indicating that guanosine-induced anti-apoptosis is mediated by GPCR22 as indicated by Caspase-3 activation.

Example 11: Ca²⁺ Determination and Quantification Experiments

Loading of Cells with Fluo-4:

Fluo-4 AM calcium imaging was used to visualize intracellular calcium concentration in the GPRC22-transfected and non-transfected S2 cells. A 2.5 mM stock solution of Fluo-4 Am dye (molecular Probes, Burlington, ON) was prepared in DMSO and 20% Pluronic F-127 and used to within a week. The S2 cell preparations were incubated with a final concentration of 5 μM fluo-4AM and 0.02% Pluronic F-127 in 1 ml S2 culture medium for 20 min at room temperature, then washed to allow for full de-esterification of AM esters. Imaging was carried out on an upright Nikon Eclipse FN-S2N upright fluorescence microscope using 10×/40× objectives with a filter to excite Fluo-4, a dye at 488 nm wavelength (peak excitation=494 nm and peak emission=516 nm) using a Lambda DG-4 illuminator (Sutter Instrument Co., Novato, Calif., USA). Images were captured using a Quantem 512SC camera with a frame rate of 5-10 frames per second and Nikon-NIS Elements, advanced research, imaging software.

Intracellular calcium concentration was created in the Nikon-NIS elements program using regions of interest (ROIs) per each experiment. ROIs were selected free hand and encompassed the cell body to be analyzed. The ROIs were tracked and the average pixel intensity was measured in that region for the duration of the recording. These measurements were then exported to Excel and Clampfit for further analysis of frequency and amplitude.

Intracellular calcium concentration of S2 cells was monitored at room temperature. 20-30 S2 cells were calculated to determine the average overall fluorescence signal intracellular calcium concentration. The fluorescence intensity was presented as the ratio F1/F0 in which the raw fluorescence intensity signals of a region of interest (ROI) was compared to the first fluorescence signal in that ROI throughout the recording. The Wilcoxon matched pairs t-test was used on two samples with equal variances to determine statistically significant differences at P=0.05. In each set of experiments, the exposure protocols for control and test conditions were identical. The results are shown in FIG. 15 where exogenously added guanosine is shown to elevate intracellular Ca²⁺ levels.

Example 12: Guanosine-Induced Elevation of Intracellular Ca²⁺ Levels is Mediated by GPCR22

Effects of Guanosine Binding GPCR22 on the Intracellular Concentration of Ca²⁺ ([Ca²⁺]i):

FIG. 12a shows the effects of guanosine on intracellular Ca²⁺ levels in normal, non-GPCR22 transfected cells, whereas FIG. 12b shows the effect of guanosine on intracellular Ca²⁺ levels in S2 cells expressing GPCR22. Both FIG. 12a and FIG. 12b are fluorescence images showing intracellular Ca²⁺ levels. It is clear from FIG. 12a and FIG. 12b that guanosine acts on GPCR22 to elevate intracellular Ca²⁺ levels. FIG. 12c graphically shows guanosine-induced [Ca2+]i increase in transfected S2 cells expressing the GPCR22 receptor and FIG. 12d shows that guanosine does not induce a [Ca2-F]i increase in normal S2 cells. No significant difference of the intracellular calcium concentration on non-transfected S2 cells between vehicle treated and guanosine treated S2 cells were noted. Data are mean+/−SEM. *P<0.05, **P<0.001. Data are representative of at least 20 cells in each group. Scale bar=200 μm.

Effects of Guanosine Binding GPCR22 on the Intracellular Concentration of Ca²⁺ ([Ca²+]i) when Measured Immediately after Adding Guanosine:

FIGS. 13a to d show the sequence calcium imaging at time points 0 min, 0.5 min, 1 min and 2 min recording, respectively. Accordingly, a fast and transient fluorescence increase in intracellular Ca²⁺ after guanosine (100 μM) addition to GPCR22-transfected S2 cells was observed. FIG. 13e shows a significant increase in intracellular Ca²⁺ in GPCR22-transfected S2 cells following guanosine (25 μM) addition (at time point-1 min recording). FIG. 13f shows no significant difference after high dose guanosine (25 μM-400 μM) addition to GPCR22-transfected S2 cells, at time point-1 min recording. FIG. 13g shows a time course of low dose (0.1 μM to 10 μM) guanosine-induced [Ca2+]i increase in GPCR22-transfected 82 cells.

The data shows that guanosine significantly increases intracellular calcium level in GPCR22-transfected S2 cells in time (within 2 mins. after adding guanosine) and in a dose-depend manner (peak with 5 μM), while it had no effect on the calcium level of non-transfected S2 cells. This indicates that guanosine-dependent intracellular level of Ca²⁺ elevation is dependent on and meditated by the GPCR22 receptor.

Example 13: GPCR22 Binding Using Radioactive Labeled Guanosine

The ability of GPCR22 receptor to bind to guanosine was assessed by performing competitive binding studies in the presence of cold guanosine. GPCR22 protein extracted from transfected 82 cells were used in performing receptor-binding studies. The binding of [³H]-guanosine (“hot” guanosine) to GPCR22 receptor was performed in triplicate in a final volume of 125 μl assay buffer (pH 7.4, 50 mM Tris-HCl, 1 mM EDTA, 5 mM MgCl2, 0.1 mM DTT, 0.1 mM PMSF, 100 mg/ml bacitracin and 5 mg/ml soybean trypsin inhibitor) containing 10 nM [³H]-guanosine and the following concentrations of unlabeled guanosine (“cold” guanosine) (0.01 μM, 0.1 μM, 1.0 μM, 10 μM, 100 μM and 1 mM) and 50 ug of protein. The incubation of the GPCR22 receptor protein with ligands was carried out at 25° C. for 75 min. At the end of the incubation period, the unbound ligands were separated by vacuum filtration through Whatman GF/B filters. The bound ligand-protein was further washed 3 times with 5 ml of Tris-EDTA buffer, pH 7.4 (50 mM Tris-HCl, 1 mM EDTA). The radioactive filters were placed in plastic counting vials containing 4 ml of scintillation fluid, equilibrated overnight in a dark environment and counted the next day in a Beckman LS5000 liquid scintillation counter Model 1780. Non-specific binding was also calculated by the addition of excess guanosine (10 mM).

[³H]-Guanosine Binding Study:

The competition studies of the [³H]-guanosine with unlabeled guanosine (cold) show that guanosine binds to GPCR22 in a single high affinity binding site with a KD of 170.9±39.79 nM and Bmax of 1.05±0.12 pmol mg⁻¹ protein as shown in FIG. 14. The FIG. 14 saturation curve analysis results are as follows:

Specific Binding Protein

Equation 1

Variables: BMAX=1.057; KD=170.9

Std. Error: BMAX=0.1207; KD=39.79

95% Confidence Intervals: BMAX=0.8038 to 1.311; KD=87.26 to 254.5

Goodness of Fit: Degrees of Freedom=18; R²=0.9493; Absolute Sum of

Squares=0.05014; Sy.x=0.05278

Data: Number of X values=8; Number of Y replicates=3; Total number of values=20; Number of missing values=4.

Accordingly, it has been shown that GPCR22 has a high-affinity binding site for guanosine.

Therefore, in light of above, it has been surprisingly discovered that the previously orphaned G-Protein Coupled Receptor 22 (GPCR22) is able to bind guanosine and is a cell-surface receptor therefor. Accordingly, cell-types devoid of this receptor may be transfected to express GPCR22 for use in screening of guanosine analogues and or ligand to the GPRC22 receptor for various medical, non-medical and research purposes. Additionally, transformed cells lines expressing GPCR22 may also be stably cultured for use in such experiments, among other uses. For example, in the embodiments disclosed herein, although not wishing to be limited thereto, 1321N1 human astrocytoma cells and Drosophila Schneider 2 cells may be transfected and made into transformed cell lines to express the GPCR22 receptor which is not otherwise endogenously expressed in the non-transfected counterparts of these cells. Other cell types may be readily apparent to one of skill in art from a reading of the techniques disclosed herein and may also be transfected to express GPCR22.

It is to be understood that the above description it is intended to be illustrative, and not restrictive. Many other embodiments will be apparent to those skilled in the art, upon reviewing the above description. The scope of the invention should, therefore, be determined with reference to the appended claims, along with the full scope of equivalents to which such claims are entitled.

Although the present invention has been described with reference to specific exemplary embodiments, it will be evident that various modifications and changes may be made to these embodiments without departing from the broader spirit and scope of the disclosed subject matter as defined by the appended claims. 

What is claimed is: 1) A transformed cell line expressing a non-endogenous G-Protein Coupled Receptor, said transformed cell line proliferated from a host cell having been transformed by transfection with a recombinant cDNA sequence coding for an amino acid sequence having at least 70% identity to SEQ. ID NO: 3 so as to express a cell-surface G-Protein Coupled Receptor able to bind Guanosine and Guanosine analogs. 2) The transformed cell line as defined in claim 1, wherein said recombinant cDNA sequence comprises SEQ. ID NO: 1 or SEQ. ID NO:
 2. 3) The transformed cell line as defined in claim 1, wherein said amino acid sequence comprises SEQ. ID NO:
 3. 4) The transformed cell line as defined in claim 1, said amino acid sequence having at least 80% identity to SEQ. ID NO:
 3. 5) The transformed cell line as defined in claim 1, said amino acid sequence having at least 90% identity to SEQ. ID NO:
 3. 6) The transformed cell line as defined in claim 1, said amino acid sequence having at least 95% identity to SEQ. ID NO:
 3. 7) The transformed cell line as defined in claim 1, wherein said host cell is a Drosophila Schneider 2 cell or a human astrocytoma 1321N1 cell. 8) A method for producing the transformed cell line as defined claim 1 comprising: transfecting said host cell with an expression vector, said expression vector comprising a polynucleotide, said polynucleotide comprising a nucleotide sequence encoding a polypeptide comprising an amino acid sequence having at least 70% identity to SEQ. ID NO.
 3. 9) A method for identifying a compound bindable to a selective Guanosine responsive G-Protein Coupled Receptor comprising: contacting one or more candidate compounds with a host cell transformed to express a receptor comprising an amino acid sequence having at least 70% identity to SEQ. ID NO: 3; and measuring the ability of the one or more candidate compounds to stimulate or inhibit a cellular function associated with said receptor. 10) The method as defined in claim 9, wherein said amino acid sequence is encoded by DNA comprising SEQ. ID NO: 1 or SEQ. ID NO:
 2. 11) The method as defined in claim 9, wherein said stimulation or inhibition is indicative of a compound for regulating apoptosis, intracellular calcium mobilization, intracellular protein phosphorylation or a second messenger intracellular pathway. 12) The method as defined in claim 9, wherein said stimulation or inhibition is indicative of a compound for regulating apoptosis, intracellular calcium mobilization, intracellular protein phosphorylation or a second messenger intracellular pathway. 13) The method as defined in claim 9, wherein said host cell is a Drosophila Schneider 2 cell or a human astrocytoma 1321N1 cell. 14) The method as defined in claim 9, wherein said one or more candidate compounds which regulates apoptosis, intracellular calcium mobilization, intracellular protein phosphorylation or a second messenger intracellular pathway is an agonist, a partial agonist or an inverse agonist of the receptor. 15) A method for transforming a host cell to express a Guanosine bindable G-Protein Coupled receptor, the method comprising: transfecting a host cell with an expression vector, said expression vector comprising a polynucleotide sequence comprising SEQ. ID NO: 1 or SEQ. ID NO: 2, encoding for a polypeptide comprising an amino acid sequence comprising SEQ. ID NO: 3; wherein said host cell under the appropriate culture conditions, produces a polypeptide comprising said amino acid sequence of SEQ. ID NO:
 3. 16) The method as defined in claim 15, wherein the polypeptide comprising SEQ. ID NO: 3 corresponds to GPCR22 and is expressed at the cell surface. 17) The method as defined in claim 16, wherein said host cell is a Drosophila Schneider 2 cell or a human astrocytoma 1321N1 cell. 18) A transformed cell line expressing a non-endogenous G-Protein Coupled Receptor capable of binding guanosine or analogues thereof, said non-endogenous G-Protein Coupled Receptor having a guanosine or analogue thereof binding domain located in transmembrane domain 6, said binding domain comprising SEQ. ID NO: 7 or SEQ. ID NO:
 8. 19) The transformed cell line as defined in either one of claim 18, wherein said transformed cell line is resultant from a Drosophila Schneider 2 host cell or a human astrocytoma 1321N1 host cell transfected to express GPCR22. 